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rs864309698

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864309698(A;A)
Make rs864309698(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position25229484
GeneCRYBB2
is asnp
is mentioned by
dbSNPrs864309698
ebirs864309698
HLIrs864309698
Exacrs864309698
Varsomers864309698
Maprs864309698
PheGenIrs864309698
hapmaprs864309698
1000 genomesrs864309698
hgdprs864309698
ensemblrs864309698
gopubmedrs864309698
geneviewrs864309698
scholarrs864309698
googlers864309698
pharmgkbrs864309698
gwascentralrs864309698
openSNPrs864309698
23andMers864309698
23andMe allrs864309698
SNP Nexus

SNPshotrs864309698
SNPdbers864309698
MSV3drs864309698
GWAS Ctlgrs864309698
Max Magnitude0
ClinVar
Risk rs864309698(A;A)
Alt rs864309698(A;A)
Reference rs864309698(G;G)
Significance Probable-Pathogenic
Disease Congenital cataract
Variation info
Gene CRYBB2
CLNDBN Congenital cataract
Reversed 0
HGVS NC_000022.10:g.25625451G>A
CLNSRC
CLNACC RCV000203383.1,